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CONTOURA
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CONTOURA Operator Manual
35
After each treatment session, the patient should be advised to contac
t the
physician if there is any indication of infec
tion, excessive swelling, redness, pain,
or any other unusual or untoward symptom.
34
36
Table of Contents
Main Page
Default Chapter
3
Table of Contents
3
Section 1 - Introduction
5
Before You Start
5
System Overview
5
Conventions Used in the Manual
5
Explanation of the Symbols Used on the System
6
Section 2 - Safety
7
The Patient
7
Treating Attendant
7
Cautions
8
Electrical and Mechanical Safety
8
Fire Hazards
8
Safety Operational Use of the System
8
Safe Use of the Active Accessory
9
Warnings
10
Device Labels
11
Handpiece Labels
11
Equipment Classification
14
Section 3 - System Installation
15
Electrical Requirements
15
Environmental Requirements
15
Equipment List
15
Unpackaging
16
Installation
16
Moving the System
16
Disposal of System
17
Section 4 - Description of Device
18
Rear Panel
18
Front Panel and Operator Control Panel
18
Software Screens
20
Sound Indicator
25
Cut-Off Temperature Control
25
Handpiece
26
Section 5 - System Operation
29
Device Start-Up
29
System Shutdown
29
Section 6 - Treatment Information Bodyfx/Minifx
30
Indications for Use
30
Contraindications
30
Possible Adverse Effects
31
Handpiece Cleaning Instruction Prior to Use
31
Pre-Treatment Recommendations
32
Treatment Recommendations
33
Treatment Schedule
34
Post-Treatment Recommendations
34
Section 7 - Treatment Information Forma-Plus
36
Indications for Use
36
Contraindications
36
Possible Adverse Effects
37
Handpiece Cleaning Instruction Prior to Use
37
Pre-Treatment Recommendations
38
Treatment Recommendations
39
Treatment Schedule
40
Post-Treatment Recommendations
41
Section 8- System Maintenance
42
Maintenance & Frequency
42
Before and after each Treatment
42
Once a Week
42
Once a Year
42
Section 8 - Troubleshooting
43
Description of Faults with All Handpieces
43
Section 13 - System Specifications
44
Rf Output Power Curves
45
Emc Safety for the Rf Device
45
Curve
45
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